MicroAire Surgical Instruments, LLC recalls Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry

Recall date

March 11, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1834-2016

FDA classification

Class II

Brand / firm

MicroAire Surgical Instruments, LLC

Sold / distributed

United States

Why it was recalled

MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol markings on them.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Pneumatic Impactor, General Surgery, With Microaire Hose Connector Professional Use, Medical Industry